Stability study of tyrosinate radical in a restricted phyllomorphous medium

dc.contributor.authorGournis, D.en
dc.contributor.authorDeligiannakis, Y.en
dc.contributor.authorKarakassides, M. A.en
dc.contributor.authorBoussac, A.en
dc.contributor.authorIoannidis, N.en
dc.contributor.authorPetridis, D.en
dc.date.accessioned2015-11-24T17:38:30Z
dc.date.available2015-11-24T17:38:30Z
dc.identifier.issn0743-7463-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/14503
dc.rightsDefault Licence-
dc.subjectresonance raman-spectroscopyen
dc.subjectaromatic-moleculesen
dc.subjectphotosystem-iien
dc.subjectmontmorilloniteen
dc.subjectclaysen
dc.subjectsmectiteen
dc.subjectpolymerizationen
dc.subjectinterlayeren
dc.subjecthectoriteen
dc.subjectsorptionen
dc.titleStability study of tyrosinate radical in a restricted phyllomorphous mediumen
heal.abstractThe elusive tyrosinate radical has been stabilized in the layers of synthetic laponite on intercalated tyrosinate ester molecules. According to EPR, XRD, and FT-IR data, the tyrosinate ester molecules adopt a horizontal orientation between the clay surfaces, with the aromatic rings almost perpendicular to the clay layers, giving an intersheet separation of 4.8 Angstrom. The radical remains stable for over two months, while it is quickly reduced by nitric oxide. The observed long-term stability of the radical is due to electrostatic interactions with the negative surface of the clay as well as to sequestration phenomena which protect the radical from polymerization.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1021/La026292u-
heal.identifier.secondary<Go to ISI>://000179719600061-
heal.journalNameLangmuiren
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2002-
heal.publisherAmerican Chemical Societyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Μηχανικών Επιστήμης Υλικώνel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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